Colonoscopy Training With or Without Artificial Intelligence Among Endoscopy Residents: a Randomized Controlled Study
Objectives: Primary: Adenoma Miss Rate (AMR) in the end of the first year of training for each group and after the crossover. Secondary: Further endoscopists-related parameters will be recorded and compared between the two arms: PDR, ADR, aADR, PMR, withdrawal time, CIR, AEs The investigators will be asked, when possible, to follow-up the patients until they have their next colonoscopy or a diagnosis of CRC to assess for interval cancer.
• Trial participants: Endoscopy trainees at any time of their training, with at least one year of training ahead without previous structured exposure to CADe during their training.
‣ Recruited patient population: Adult patients undergoing diagnostic, screening, or surveillance colonoscopy will be included.
⁃ Provision of signed and dated informed consent form understand the risks and benefits of the study
⁃ Aged ≥18 years old
⁃ Able to read and write in the provided language.
⁃ Participants capable to provide written informed consent and comply with the trial protocol.